Pages that link to "United States National Library of Medicine"
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The following pages link to United States National Library of Medicine:
Displaying 50 items.
- TAS2R43 (← links)
- TAS2R44 (← links)
- TAS2R45 (← links)
- TAS2R12 (← links)
- TAS2R46 (← links)
- TAS2R47 (← links)
- TAS2R48 (← links)
- TAS2R49 (← links)
- TAS2R50 (← links)
- TAS2R60 (← links)
- OPN3 (← links)
- OPN5 (← links)
- GPR176 (← links)
- LGR6 (← links)
- Prostacyclin receptor (← links)
- OR1D2 (← links)
- OXGR1 (← links)
- EBI2 (← links)
- RRH (← links)
- Retinal G protein coupled receptor (← links)
- P2RY5 (← links)
- GPR103 (← links)
- TAAR2 (← links)
- GPR77 (← links)
- GPR44 (← links)
- VN1R1 (← links)
- VN1R2 (← links)
- VN1R3 (← links)
- Prostaglandin E2 receptor (← links)
- Angiotensin II receptor type 1 (← links)
- NAD(P)H dehydrogenase (quinone 1) (← links)
- Phosphatidylethanolamine N-methyltransferase (← links)
- Aralkylamine N-acetyltransferase (← links)
- Mitogen-activated protein kinase 9 (← links)
- MAPK8 (← links)
- GATA4 (← links)
- ID2 (← links)
- SREBF2 (← links)
- MT-ATP6 (← links)
- MT-TL1 (← links)
- MT-TH (← links)
- MT-ND5 (← links)
- HTR3A (← links)
- CDKN2A (← links)
- Wikipedia:MeSH C19 (← links)
- U.S. National Library of Medicine (redirect page) (← links)
- Cystinosis (← links)
- MedlinePlus (← links)
- Von Hippel-Lindau disease (← links)
- Arginemia (← links)
- Vitelliform macular dystrophy (← links)
- Leber's hereditary optic neuropathy (← links)
- Bloom syndrome (← links)
- Chromosome 7 (human) (← links)
- 3-Methylcrotonyl-CoA carboxylase deficiency (← links)
- 3-Methylglutaconic aciduria (← links)
- 3-hydroxy-3-methylglutaryl-CoA lyase deficiency (← links)
- Carbamoyl phosphate synthetase I deficiency (← links)
- Duane-radial ray syndrome (← links)
- Emery-Dreifuss muscular dystrophy (← links)
- Ethylmalonic encephalopathy (← links)
- Fabry's disease (← links)
- Glutaric aciduria type 1 (← links)
- Glutathione synthetase deficiency (← links)
- Greig cephalopolysyndactyly syndrome (← links)
- Hereditary coproporphyria (← links)
- Holt-Oram syndrome (← links)
- Isobutyryl-coenzyme A dehydrogenase deficiency (← links)
- Isovaleric acidemia (← links)
- Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (← links)
- Malonyl-CoA decarboxylase deficiency (← links)
- Maple syrup urine disease (← links)
- Medium-chain acyl-coenzyme A dehydrogenase deficiency (← links)
- Mitochondrial trifunctional protein deficiency (← links)
- Myotonic dystrophy (← links)
- Neuropathy, ataxia, and retinitis pigmentosa (← links)
- Norrie disease (← links)
- Ornithine translocase deficiency (← links)
- Pallister-Hall syndrome (← links)
- Pyruvate carboxylase deficiency (← links)
- Short-chain acyl-coenzyme A dehydrogenase deficiency (← links)
- Spondyloepiphyseal dysplasia congenita (← links)
- Spondyloperipheral dysplasia (← links)
- Tay-Sachs disease (← links)
- Very long-chain acyl-coenzyme A dehydrogenase deficiency (← links)
- Perforin (← links)
- Medical literature retrieval (← links)
- Methylmalonic acidemia (← links)
- Sudden infant death syndrome (← links)
- Hearing loss with craniofacial syndromes (← links)
- Transmissible spongiform encephalopathy (← links)
- Erythropoietic protoporphyria (← links)
- Methylmalonyl-CoA mutase deficiency (← links)
- Hepatoerythropoietic porphyria (← links)
- Chromosome 7 (← links)
- Argininemia (← links)
- Template:NLM (← links)
- SLC5A1 (← links)
- Leptin receptor (← links)
- Wikipedia:MeSH A10 (← links)
- Ebers Papyrus (← links)